Cordypyridones E–J: Antibiofilm 2-Pyridone Alkaloids from the Nematode Antagonistic Fungus <i>Laburnicola nematophila</i>

In the course of biochemical prospection of <i>Laburnicola nematophila</i> isolated from eggs of the plant-parasitic cyst nematode <i>Heterodera filipjevi</i>, eight 2-pyridone alkaloids were isolated from its solid-state BRFT cultures and identified as six previously undescribed, cordypyridones E-J (<b>1</b>-<b>6</b>), and two known congeners, cordypyridones C (<b>7</b>) and D (<b>8</b>). The structures and absolute configurations of all isolated compounds were elucidated through HR-ESI-MS, 1D/2D NMR spectroscopy, and TDDFT-ECD calculations. Compound <b>4</b>, bearing a rare <i>N</i>-hydroxy-2-pyridone moiety structurally related to that of PF1140, exhibited broad-spectrum bioactivity in cytotoxicity and antimicrobial assays. Compounds <b>5</b> and <b>6</b> demonstrated potent antibiofilm activities against <i>Staphylococcus aureus</i>, reducing its biofilm formation by almost 50% at 0.25 and 7.8 μg/mL, respectively.

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Publication Details

Journal
Journal of Natural Products
Published
2025-10-14
DOI
https://doi.org/10.1021/acs.jnatprod.5c00768
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
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article

Cordypyridones E–J: Antibiofilm 2-Pyridone Alkaloids from the Nematode Antagonistic Fungus Laburnicola nematophila

Hedda Schrey, Jan‐Peer Wennrich, S. Fushimi, Marc Stadler et al.
Journal of Natural Products
Microbial Natural Products and Biosynthesis
article

Cordypyridones E–J: Antibiofilm 2-Pyridone Alkaloids from the Nematode Antagonistic Fungus Laburnicola nematophila

Hedda Schrey, Jan‐Peer Wennrich, S. Fushimi, Marc Stadler, Mahmoud A. A. Ibrahim, Wolfgang Maier, Sherif S. Ebada, Samad Ashrafi, Caren Holzenkamp
article en

Abstract

In the course of biochemical prospection of <i>Laburnicola nematophila</i> isolated from eggs of the plant-parasitic cyst nematode <i>Heterodera filipjevi</i>, eight 2-pyridone alkaloids were isolated from its solid-state BRFT cultures and identified as six previously undescribed, cordypyridones E-J (<b>1</b>-<b>6</b>), and two known congeners, cordypyridones C (<b>7</b>) and D (<b>8</b>). The structures and absolute configurations of all isolated compounds were elucidated through HR-ESI-MS, 1D/2D NMR spectroscopy, and TDDFT-ECD calculations. Compound <b>4</b>, bearing a rare <i>N</i>-hydroxy-2-pyridone moiety structurally related to that of PF1140, exhibited broad-spectrum bioactivity in cytotoxicity and antimicrobial assays. Compounds <b>5</b> and <b>6</b> demonstrated potent antibiofilm activities against <i>Staphylococcus aureus</i>, reducing its biofilm formation by almost 50% at 0.25 and 7.8 μg/mL, respectively.

Journal of Natural ProductsVol. 88(10)
Ain Shams University (EG), Julius Kühn-Institut (DE), University of Applied Science and Technology (IR), University of the Free State (ZA), Czech Academy of Sciences, Institute of Animal Physiology and Genetics (CZ), College of Applied Sciences, Nizwa (OM), Czech Academy of Sciences, Institute of Microbiology (CZ), Helmholtz Centre for Infection Research (DE), Institute of Molecular Genetics (RU), Computational Physics (United States) (US), Pediatrics and Genetics (US), Pharmac (NZ), Toyama Prefectural University (JP), Minia University (EG), Technische Universität Braunschweig (DE), University of KwaZulu-Natal (ZA)
Openalex Percentile: Top 67%
Microbial Natural Products and Biosynthesis
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